The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Comparative analysis of metazoan chromatin organization
Open accessAbstract
A large collection of new modENCODE and ENCODE genome-wide chromatin data sets from cell lines and developmental stages in worm, fly and human are analysed; this reveals many conserved features of chromatin organization among the three organisms, as well as notable differences in the composition and locations of repressive chromatin. This study describes numerous new genome-wide chromatin data sets from cell lines and developmental stages of Homo sapiens, Drosophila melanogaster and Caenorhabditis elegans generated by the ENCODE and modENCODE consortia. The results point to many conserved features of chromatin organization among the three organisms, while identifying differences in the composition and locations of repressive chromatin. Genome function is dynamically regulated in part by chromatin, which consists of the histones, non-histone proteins and RNA molecules that package DNA. Studies in Caenorhabditis elegans and Drosophila melanogaster have contributed substantially to our understanding of molecular mechanisms of genome function in humans, and have revealed conservation of chromatin components and mechanisms1,2,3. Nevertheless, the three organisms have markedly different genome sizes, chromosome architecture and gene organization. On human and fly chromosomes, for example, pericentric heterochromatin flanks single centromeres, whereas worm chromosomes have dispersed heterochromatin-like regions enriched in the distal chromosomal ‘arms’, and centromeres distributed along their lengths4,5. To systematically investigate chromatin organization and associated gene regulation across species, we generated and analysed a large collection of genome-wide chromatin data sets from cell lines and developmental stages in worm, fly and human. Here we present over 800 new data sets from our ENCODE and modENCODE consortia, bringing the total to over 1,400. Comparison of combinatorial patterns of histone modifications, nuclear lamina-associated domains, organization of large-scale topological domains, chromatin environment at promoters and enhancers, nucleosome positioning, and DNA replication patterns reveals many conserved features of chromatin organization among the three organisms. We also find notable differences in the composition and locations of repressive chromatin. These data sets and analyses provide a rich resource for comparative and species-specific investigations of chromatin composition, organization and function.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The median distance between the common boundaries was approximately 750 kb, consistent with the reported median TAD size in human cells4,19 (Extended Data Fig. 1e).”
From Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer (2020) · cites this paper as [19]
In the citing paper
“The obtained matrix was grouped using the k-means clustering approach and five distinct groups of TADs were identified similar to a previous classification of chromatin domains17,19,33. These groups comprised heterochromatin (61), low/quiescent (705), repressed (481), low-active (764) and active (365) domains (Fig. 4a, Supplementary Table 4).”
From Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer (2020) · cites this paper as [19]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
An integrated encyclopedia of DNA elements in the human genome
The ENCODE Project Consortium (2012) · Nature · doi:10.1038/nature11247 · Cited by 18,072
Self-citationTopological domains in mammalian genomes identified by analysis of chromatin interactions
Dixon, J. R., Selvaraj, S., Yue, F., Kim, A., Li, Y., Shen, Y., Hu, M., Liu, J. S., & Ren, B. (2012) · Nature · doi:10.1038/nature11082 · Cited by 6,829
Mapping and analysis of chromatin state dynamics in nine human cell types
Ernst, J., Kheradpour, P., Mikkelsen, T. S., Shoresh, N., Ward, L. D., Epstein, C. B., Zhang, X., Wang, L., Issner, R., Coyne, M., et al. (2011) · Nature · doi:10.1038/nature09906 · Cited by 2,898
Self-citationChIP-seq guidelines and practices of the ENCODE and modENCODE consortia
Landt, S. G., Marinov, G. K., Kundaje, A., Kheradpour, P., Pauli, F., Batzoglou, S., Bernstein, B. E., Bickel, P., Brown, J. B., Cayting, P., et al. (2012) · Genome Research · doi:10.1101/gr.136184.111 · Cited by 2,033
Self-citationThree-dimensional folding and functional organization principles of the Drosophila genome
Sexton, T., Yaffe, E., Kenigsberg, E., Bantignies, F., Leblanc, B., Hoichman, M., Parrinello, H., Tanay, A., & Cavalli, G. (2012) · Cell · doi:10.1016/j.cell.2012.01.010 · Cited by 1,983
Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE
Roy, S., Ernst, J., Kharchenko, P. V., Kheradpour, P., Nègre, N., Eaton, M. L., Landolin, J. M., Bristow, C. A., Ma, L., Lin, M. F., et al. (2010) · Science · doi:10.1126/science.1198374 · Cited by 1,242
Self-citationIntegrative Analysis of the Caenorhabditis elegans Genome by the modENCODE Project
Gerstein, M., Lu, Z. J., Nostrand, E. L. V., Cheng, C., Arshinoff, B. I., Liu, T., Yip, K. Y.-L., Robilotto, R., Rechtsteiner, A., Ikegami, K., et al. (2010) · Science · doi:10.1126/science.1196914 · Cited by 973
Self-citationComprehensive analysis of the chromatin landscape in Drosophila melanogaster
Kharchenko, P. V., Alekseyenko, A. A., Schwartz, Y. B., Minoda, A., Riddle, N. C., Ernst, J., Sabo, P. J., Larschan, E., Gorchakov, A. A., Gu, T., et al. (2010) · Nature · doi:10.1038/nature09725 · Cited by 893
Self-citationDistinct epigenomic landscapes of pluripotent and lineage-committed human cells
Hawkins, R. D., Hon, G. C., Lee, L. K., Ngo, Q., Lister, R., Pelizzola, M., Edsall, L. E., Kuan, S., Luu, Y., Klugman, S., et al. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.03.018 · Cited by 806
Step-wise methylation of histone H3K9 positions heterochromatin at the nuclear periphery
Towbin, B. D., González-Aguilera, C., Sack, R., Gaidatzis, D., Kalck, V., Meister, P., Askjaer, P., & Gasser, S. M. (2012) · Cell · doi:10.1016/j.cell.2012.06.051 · Cited by 597
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 389
Libbrecht, M. W., Rodriguez, O. L., Weng, Z., Bilmes, J. A., Hoffman, M. M., & Noble, W. S. (2019) · Genome biology · doi:10.1186/s13059-019-1784-2 · Cited by 59
Self-citationhiHMM: Bayesian non-parametric joint inference of chromatin state maps
Sohn, K.-A., Ho, J. W. K., Djordjevic, D., Jeong, H.-H., Park, P. J., & Kim, J. H. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btv117 · Cited by 45
Self-citationRyu, T., Bonner, M. R., & Chiolo, I. (2016) · Nucleus · doi:10.1080/19491034.2016.1239683 · Cited by 49
Stefano, M. D., Nützmann, H., Martı́-Renom, M. A., & Jost, D. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkaa1275 · Cited by 48
Mar, D., Gharib, S. A., Zager, R. A., Johnson, A. C. M., Denisenko, O. N., & Bomsztyk, K. (2015) · Kidney International · doi:10.1038/ki.2015.164 · Cited by 50
From single genes to entire genomes: the search for a function of nuclear organization
Pueschel, R., Coraggio, F., & Meister, P. (2016) · Development · doi:10.1242/dev.129007 · Cited by 52
And yet, it moves: nuclear and chromatin dynamics of a heterochromatic double-strand break
Caridi, P. C., Delabaere, L., Zapotoczny, G., & Chiolo, I. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0291 · Cited by 51
Regulation of Crossover Frequency and Distribution during Meiotic RecombinationPreprint
Saito, T. T., & Colaiácovo, M. P. (2017) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2017.82.034132 · Cited by 53
The appeasement of Doug: a synthetic approach to enhancer biology
Vincent, B. J., Estrada, J., & DePace, A. H. (2016) · Integrative Biology · doi:10.1039/c5ib00321k · Cited by 49
Genetic Marker Discovery in Complex Traits: A Field Example on Fat Content and Composition in Pigs
Pena, R. N., Ros‐Freixedes, R., Tör, M., & Estany, J. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17122100 · Cited by 48
Defining B Cell Chromatin: Lessons from EBF1.
Boller, S., Li, R., & Grosschedl, R. (2018) · Trends in Genetics · doi:10.1016/j.tig.2017.12.014 · Cited by 44
Janssen, A., Colmenares, S. U., Lee, T., & Karpen, G. H. (2018) · Genes & Development · doi:10.1101/gad.317537.118 · Cited by 48
Self-citationFunctions of HP1 proteins in transcriptional regulation
Schoelz, J. M., & Riddle, N. C. (2022) · Epigenetics & Chromatin · doi:10.1186/s13072-022-00453-8 · Cited by 41
Self-citationHemberger, M., & Dean, W. (2023) · Physiological Reviews · doi:10.1152/physrev.00001.2023 · Cited by 48
Ontology application and use at the ENCODE DCC
Malladi, V. S., Erickson, D. T., Podduturi, N. R., Rowe, L. D., Chan, E. T., Davidson, J. M., Hitz, B. C., Ho, M., Lee, B. T., Miyasato, S. R., et al. (2015) · Database · doi:10.1093/database/bav010 · Cited by 45
Charting the cis-regulome of activated B cells by coupling structural and functional genomics
Chaudhri, V. K., Dienger-Stambaugh, K., Wu, Z., Shrestha, M., & Singh, H. (2018) · Nature Immunology · doi:10.1038/s41590-019-0565-0 · Cited by 46
Deep homology in the age of next-generation sequencing
Tschopp, P., & Tabin, C. J. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0475 · Cited by 45
Evolution of holocentric chromosomes: Drivers, diversity, and deterrents
Senaratne, A. P., Cortes-Silva, N., & Drinnenberg, I. A. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.01.003 · Cited by 44
H3K23me2 is a new heterochromatic mark in Caenorhabditis elegans
Vandamme, J., Sidoli, S., Mariani, L. L., Friis, C., Christensen, J. F., Helin, K., Jensen, O. N., & Salcini, A. E. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1063 · Cited by 44
Esposito, A., Bianco, S., Chiariello, A. M., Abraham, A., Fiorillo, L., Conte, M., Campanile, R., & Nicodemi, M. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110601 · Cited by 47
Kasinathan, B., Colmenares, S. U., McConnell, H., Young, J. M., Karpen, G. H., & Malik, H. S. (2020) · eLife · doi:10.7554/elife.63368 · Cited by 41
Self-citationMoore, B. L., Aitken, S., & Semple, C. A. M. (2015) · Genome biology · doi:10.1186/s13059-015-0661-x · Cited by 40
Chen, Y., Wang, Y., Xuan, Z., Chen, M., & Zhang, M. Q. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw225 · Cited by 41
Cytosine Methylation Affects the Mutability of Neighboring Nucleotides in Germline and Soma
Kusmartsev, V., Dróżdż, M., Schuster‐Böckler, B., & Warnecke, T. (2020) · Genetics · doi:10.1534/genetics.120.303028 · Cited by 42
Coupling 1D modifications and 3D nuclear organization: data, models and function
Jost, D., Vaillant, C., & Meister, P. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.12.001 · Cited by 42
Urban, J. A., Kuzu, G., Bowman, S., Scruggs, B. S., Henriques, T., Kingston, R. E., Adelman, K., Tolstorukov, M. Y., & Larschan, E. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186855 · Cited by 40
Self-citationDiversification of the Caenorhabditis heat shock response by Helitron transposable elements
Garrigues, J. M., Tsu, B. V., Daugherty, M. D., & Pasquinelli, A. E. (2019) · eLife · doi:10.7554/elife.51139 · Cited by 37
Self-citationPolytene Chromosomes – A Portrait of Functional Organization of the Drosophila Genome
Zykova, T. Y., Levitsky, V. G., Belyaeva, E. S., & Zhimulev, I. F. (2017) · Current Genomics · doi:10.2174/1389202918666171016123830 · Cited by 39
Busby, M., Xue, C., Li, C., Farjoun, Y., Gienger, E., Yofe, I., Gladden, A. D., Epstein, C. B., Cornett, E. M., Rothbart, S. B., et al. (2016) · Epigenetics & Chromatin · doi:10.1186/s13072-016-0100-6 · Cited by 42
Self-citationEpigenetic Factors that Control Pericentric Heterochromatin Organization in Mammals
Fioriniello, S., Marano, D., Fiorillo, F., D’Esposito, M., & Ragione, F. D. (2020) · Genes · doi:10.3390/genes11060595 · Cited by 39
Nucleic Acids Persistence—Benefits and Limitations in Forensic Genetics
Żarczyńska, M., Żarczyński, P., & Tomsia, M. (2023) · Genes · doi:10.3390/genes14081643 · Cited by 43
3D spatial genome organization in the nervous system: From development and plasticity to disease
Fujita, Y., Pather, S. R., Ming, G., & Song, H. (2022) · Neuron · doi:10.1016/j.neuron.2022.06.004 · Cited by 37
Genome architecture: from linear organisation of chromatin to the 3D assembly in the nucleus
Sequeira‐Mendes, J., & Gutiérrez, C. (2015) · Chromosoma · doi:10.1007/s00412-015-0538-5 · Cited by 36
On the Regulatory Evolution of New Genes Throughout Their Life History
Zhang, J., & Zhou, Q. (2018) · Molecular Biology and Evolution · doi:10.1093/molbev/msy206 · Cited by 36
Is There a Histone Code for Cellular Quiescence?
Bonitto, K., Sarathy, K., Atai, K., Mitra, M., & Coller, H. A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.739780 · Cited by 39
Regulation of the BMP Signaling-Responsive Transcriptional Network in the Drosophila Embryo
Deignan, L., Pinheiro, M. T., Sutcliffe, C., Saunders, A., Wilcockson, S. G., Zeef, L. A. H., Donaldson, I. J., & Ashe, H. L. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006164 · Cited by 39
The folding landscape of the epigenome
Olarte-Plata, J. D., Haddad, N., Vaillant, C., & Jost, D. (2016) · Physical Biology · doi:10.1088/1478-3975/13/2/026001 · Cited by 38
Buchberger, E., Reis, M., Lu, T.-H., & Posnien, N. (2019) · Genes · doi:10.3390/genes10070492 · Cited by 34
Hong, C., Lalsiamthara, J., Ren, J., Sang, Y., & Aballay, A. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001169 · Cited by 32
Carlier, F., Li, M., Maroc, L., Debuchy, R., Souaid, C., Noordermeer, D., Grognet, P., & Malagnac, F. (2021) · Epigenetics & Chromatin · doi:10.1186/s13072-021-00395-7 · Cited by 32
DNA replication through a chromatin environment
Bellush, J. M., & Whitehouse, I. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0287 · Cited by 37
NucPosDB: a database of nucleosome positioning in vivo and nucleosomics of cell-free DNA
Shtumpf, M., Piroeva, K. V., Agrawal, S. P., Jacob, D. R., & Teif, V. B. (2022) · Chromosoma · doi:10.1007/s00412-021-00766-9 · Cited by 34
Determinants of promoter and enhancer transcription directionality in metazoans
Ibrahim, M. M., Karabacak, A., Glahs, A., Kolundzic, E., Hirsekorn, A., Carda, A., Tursun, B., Zinzen, R., Lacadie, S., & Ohler, U. (2018) · Nature Communications · doi:10.1038/s41467-018-06962-z · Cited by 35
Rechtsteiner, A., Costello, M. E., Egelhofer, T. A., Garrigues, J. M., Strome, S., & Petrella, L. N. (2019) · Genetics · doi:10.1534/genetics.118.301878 · Cited by 32
Self-citationCohesin organizes 3D DNA contacts surrounding active enhancers in C. elegansPreprint
Kim, J., Wang, H., & Ercan, S. (2025) · Genome Research · doi:10.1101/gr.279365.124 · Cited by 31
Self-citationRole of the cytoskeleton in cellular reprogramming: effects of biophysical and biochemical factors
Momotyuk, E., Ebrahim, N., Shakirova, K. S., & Dashinimaev, E. B. (2025) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2025.1538806 · Cited by 31
Siahpirani, A. F., Ay, F., & Roy, S. (2016) · Genome biology · doi:10.1186/s13059-016-0962-8 · Cited by 31
LSM2-8 and XRN-2 contribute to the silencing of H3K27me3-marked genes through targeted RNA decay
Mattout, A., Gaidatzis, D., Padeken, J., Schmid, C. D., Aeschimann, F., Kalck, V., & Gasser, S. M. (2020) · Nature Cell Biology · doi:10.1038/s41556-020-0504-1 · Cited by 31
Ash1 counteracts Polycomb repression independent of histone H3 lysine 36 methylation
Dorafshan, E., Kahn, T. G., Glotov, A., Savitsky, M., Walther, M., Reuter, G., & Schwartz, Y. B. (2019) · EMBO Reports · doi:10.15252/embr.201846762 · Cited by 31
Self-citationNguyen, Q. H., Tellam, R. L., Naval-Sánchez, M., Porto-Neto, L. R., Barendse, W., Reverter, A., Hayes, B. J., Kijas, J., & Dalrymple, B. P. (2018) · GigaScience · doi:10.1093/gigascience/gix136 · Cited by 29
Heurteau, A., Perrois, C., Depierre, D., Fosseprez, O., Humbert, J., Schaak, S., & Cuvier, O. (2020) · Genome biology · doi:10.1186/s13059-020-02106-z · Cited by 32
Li, Y., Armstrong, R. L., Duronio, R. J., & MacAlpine, D. M. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw333 · Cited by 29
Self-citationRen, J.-K., Finney, R., Ni, K., Cam, M., & Muegge, K. (2019) · Epigenetics · doi:10.1080/15592294.2019.1582275 · Cited by 32
FLInt: single shot safe harbor transgene integration via F luorescent L andmark Int erference
Malaiwong, N., Porta-de-la-Riva, M., & Krieg, M. (2023) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkad041 · Cited by 28
The Renaissance of Developmental Biology
Johnston, D. S. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002149 · Cited by 30
Sex-specific chromatin landscapes in an ultra-compact chordate genome
Navrátilová, P., Danks, G., Long, A., Butcher, S., Manak, J. R., & Thompson, E. M. (2017) · Epigenetics & Chromatin · doi:10.1186/s13072-016-0110-4 · Cited by 29
Leung, W., Shaffer, C. D., Chen, E. J., Quisenberry, T. J., Ko, K., Braverman, J. M., Giarla, T. C., Mortimer, N. T., Reed, L. K., Smith, S. T., et al. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.117.040907 · Cited by 27
Khan, A., Eikani, C. K., Khan, H., Iavarone, A. T., & Pesavento, J. J. (2017) · Journal of Proteome Research · doi:10.1021/acs.jproteome.7b00780 · Cited by 28
Bautista, N. M., Crespel, A., Crossley, J. L., Padilla, P. A., & Burggren, W. W. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.222224 · Cited by 28
Campos, T. D. L., Korhonen, P. K., Hofmann, A., Gasser, R. B., & Young, N. D. (2021) · Biotechnology Advances · doi:10.1016/j.biotechadv.2021.107822 · Cited by 28
Abdulla, A. Z., Vaillant, C., & Jost, D. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac702 · Cited by 26
RNA-DamID reveals cell-type-specific binding of roX RNAs at chromatin-entry sites
Cheetham, S. W., & Brand, A. H. (2017) · Nature Structural & Molecular Biology · doi:10.1038/s41594-017-0006-4 · Cited by 27
Epigenetic Control of a Local Chromatin Landscape
Chiarella, A. M., Lu, D., & Hathaway, N. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21030943 · Cited by 31
Actin’ between phase separated domains for heterochromatin repair
Rawal, C. C., Caridi, C. P., & Chiolo, I. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102646 · Cited by 25
Arp2/3 and Unc45 maintain heterochromatin stability in Drosophila polytene chromosomes
Dialynas, G. K., Delabaere, L., & Chiolo, I. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219862282 · Cited by 26
Rodríguez-Carballo, E., Lopez‐Delisle, L., Yakushiji‐Kaminatsui, N., Ullate‐Agote, A., & Duboule, D. (2019) · BMC Biology · doi:10.1186/s12915-019-0677-x · Cited by 22
Cohesin forms fountains at active enhancers in C. elegans
Lüthi, B. N., Semple, J. I., Haemmerli, A., Thapliyal, S., Ghadage, K., Stojanovski, K., D’Asaro, D., Das, M., Gilbert, N., Glauser, D. A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-67302-6 · Cited by 28
Degradation in forensic trace DNA samples explored by massively parallel sequencing
Hanssen, E. N., Lyle, R., Egeland, T., & Gill, P. (2017) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2017.01.002 · Cited by 26
Region-specific H3K9me3 gain in aged somatic tissues in Caenorhabditis elegans
Li, C.-L. F., Pu, M., Wang, W., Chaturbedi, A., Emerson, F. J., & Lee, S. S. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009432 · Cited by 22
Self-citationSidoli, S., Vandamme, J., Salcini, A. E., & Jensen, O. N. (2015) · PROTEOMICS · doi:10.1002/pmic.201500285 · Cited by 24
Broad Chromatin Domains: An Important Facet of Genome Regulation
Carelli, F. N., Sharma, G., & Ahringer, J. (2017) · BioEssays · doi:10.1002/bies.201700124 · Cited by 24
Self-citationHuang, X., Pan, Q., Lin, Y., Gu, T., & Li, Y. (2020) · Plant Methods · doi:10.1186/s13007-020-0556-z · Cited by 24
Self-citationSemi-nonparametric modeling of topological domain formation from epigenetic data
Sefer, E., & Kingsford, C. (2019) · Algorithms for Molecular Biology · doi:10.1186/s13015-019-0142-y · Cited by 23
Caridi, C. P., Delabaere, L., Tjong, H., Hopp, H. E., Das, D., Alber, F., & Chiolo, I. (2018) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2017.11.033 · Cited by 20
Predicting gene essentiality in Caenorhabditis elegans by feature engineering and machine-learning
Campos, T. D. L., Korhonen, P. K., Sternberg, P. W., Gasser, R. B., & Young, N. D. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.05.008 · Cited by 23
Jeffers, T. E., & Lieb, J. D. (2016) · Genome Research · doi:10.1101/gr.208173.116 · Cited by 23
Self-citationChromatin organization changes during the establishment and maintenance of the postmitotic state
Ma, Y., & Buttitta, L. (2017) · Epigenetics & Chromatin · doi:10.1186/s13072-017-0159-8 · Cited by 22
Yang, B., Xu, X., Russell, L., Sullenberger, M. T., Yanowitz, J. L., & Maine, E. M. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1007992 · Cited by 22
Engineering Multidimensional Evolutionary Forces to Combat Cancer
McCoach, C. E., & Bivona, T. G. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-18-1196 · Cited by 23
Bianco, S., Annunziatella, C., Andrey, G., Chiariello, A. M., Esposito, A., Fiorillo, L., Prisco, A., Conte, M., Campanile, R., & Nicodemi, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.013 · Cited by 25
Implicating candidate genes at GWAS signals by leveraging topologically associating domains
Way, G. P., Youngstrom, D. W., Hankenson, K. D., Greene, C. S., & Grant, S. F. A. (2017) · European Journal of Human Genetics · doi:10.1038/ejhg.2017.108 · Cited by 21
Ferraro, A. R., Ameri, A. J., Lu, Z., Kamei, M., Schmitz, R. J., & Lewis, Z. (2021) · BMC Genomics · doi:10.1186/s12864-021-07774-0 · Cited by 21
A ChIP on the shoulder? Chromatin immunoprecipitation and validation strategies for ChIP antibodies
Wardle, F. C., & Tan, H. (2015) · F1000Research · doi:10.12688/f1000research.6719.1 · Cited by 22
Recurrent Gene Duplication Diversifies Genome Defense Repertoire in Drosophila
Levine, M. T., Wende, H. V., Hsieh, E., Baker, E. P., & Malik, H. S. (2016) · Molecular Biology and Evolution · doi:10.1093/molbev/msw053 · Cited by 19
Fiorillo, L., Bianco, S., Esposito, A., Conte, M., Sciarretta, R., Musella, F., & Chiariello, A. M. (2019) · Wiley Interdisciplinary Reviews Computational Molecular Science · doi:10.1002/wcms.1454 · Cited by 24
Wang, K., Dai, R., Xia, Y., Tian, J., Jiao, C., Mikhailova, T., Zhang, C., Chen, C., & Liu, C. (2021) · Epigenetics · doi:10.1080/15592294.2021.1993607 · Cited by 23
Serebreni, L., Pleyer, L., Haberle, V., Hendy, O., Vlasova, A. V., Loubière, V., Nemčko, F., Bergauer, K., Roitinger, E., Mechtler, K., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2023113519 · Cited by 20
Padhi, B., Reddy, D. S., & Mohapatra, D. K. (2015) · RSC Advances · doi:10.1039/c5ra17646h · Cited by 20
Kazemian, M., Ren, M., Lin, J., Liao, W., Spolski, R. J., & Leonard, W. J. (2015) · Molecular Systems Biology · doi:10.15252/msb.156172 · Cited by 20
Nucleosome-level 3D organization of the genome
Ohno, M., Priest, D. G., & Taniguchi, Y. (2018) · Biochemical Society Transactions · doi:10.1042/bst20170388 · Cited by 20
Mi-2/NuRD complex protects stem cell progeny from mitogenic Notch signaling
Zacharioudaki, E., Sanjuan, J. F., & Bray, S. J. (2019) · eLife · doi:10.7554/elife.41637 · Cited by 20
Stutzman, A. V., Liang, A. S., Beilinson, V., & Ikegami, K. (2020) · Epigenetics & Chromatin · doi:10.1186/s13072-019-0325-2 · Cited by 20
Self-citationGalan, S., Serra, F., & Martı́-Renom, M. A. (2022) · NAR Genomics and Bioinformatics · doi:10.1093/nargab/lqac021 · Cited by 18
3D genome organisation in Drosophila
Moretti, C., Stévant, I., & Ghavi-Helm, Y. (2019) · Briefings in Functional Genomics · doi:10.1093/bfgp/elz029 · Cited by 19
Lam, U. T. F., & Chen, E. S. (2022) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2021.106155 · Cited by 19
DANIO-CODE: Toward an Encyclopedia of DNA Elements in Zebrafish
Tan, H., Onichtchouk, D., & Winata, C. L. (2015) · Zebrafish · doi:10.1089/zeb.2015.1179 · Cited by 19
Kłosin, A., Reis, K., Hidalgo-Carcedo, C., Casas, E., Vavouri, T., & Lehner, B. (2017) · Science Advances · doi:10.1126/sciadv.1701143 · Cited by 17
Albini, S., Zakharova, V., & Ait‐Si‐Ali, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814879-2.00003-0 · Cited by 22
Zhang, L., Xu, M., Zhang, W., Zhu, C., Cui, Z., Fu, H., Ma, Y., Huang, S., Cui, J., Liang, S., et al. (2023) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-022-00409-6 · Cited by 18
Godbole, A. A., Gopalan, S., Nguyen, T.-K., Munden, A. L., Lui, D. S., Fanelli, M. J., Vo, P., Lewis, C. A., Spinelli, J. B., Fazzio, T. G., et al. (2023) · eLife · doi:10.7554/elife.79511 · Cited by 16
Metadata
- Authors
- Ho, J. W. K., Jung, Y. L., Liu, T., Alver, B. H., Lee, S., Ikegami, K., Sohn, K.-A., Minoda, A., Tolstorukov, M. Y., Appert, A., Parker, S. C. J., Gu, T., Kundaje, A., Riddle, N. C., Bishop, E., Egelhofer, T. A., Hu, S. S., Alekseyenko, A. A., Rechtsteiner, A., Asker, D., Belsky, J. A., Bowman, S. K., Chen, Q. B., Chen, R. A.-J., Day, D. S., Dong, Y., Dose, A. C., Duan, X., Epstein, C. B., Ercan, S., Feingold, E. A., Ferrari, F., Garrigues, J. M., Gehlenborg, N., Good, P. J., Haseley, P., He, D., Herrmann, M., Hoffman, M. M., Jeffers, T. E., Kharchenko, P. V., Kolasinska-Zwierz, P., Kotwaliwale, C. V., Kumar, N., Langley, S. A., Larschan, E. N., Latorre, I., Libbrecht, M. W., Lin, X., Park, R., Pazin, M. J., Pham, H. N., Plachetka, A., Qin, B., Schwartz, Y. B., Shoresh, N., Stempor, P., Vielle, A., Wang, C., Whittle, C. M., Xue, H., Kingston, R. E., Kim, J. H., Bernstein, B. E., Dernburg, A. F., Pirrotta, V., Kuroda, M. I., Noble, W. S., Tullius, T. D., Kellis, M., MacAlpine, D. M., Strome, S., Elgin, S. C. R., Liu, X. S., Lieb, J. D., Ahringer, J., Karpen, G. H., & Park, P. J.
- Affiliations
- Brigham and Women's Hospital (US)
- Harvard University (US)
- University of North Carolina at Chapel Hill (US)
- Seoul National University (KR)
- Lawrence Berkeley National Laboratory (US)
- University of Cambridge (GB)
- National Institutes of Health (US)
- Washington University in St. Louis (US)
- Broad Institute (US)
- Victor Chang Cardiac Research Institute (AU)
- Boston University (US)
- University of California, Santa Cruz (US)
- Rutgers, The State University of New Jersey (US)
- Duke Medical Center (US)
- Tongji University (CN)
- University of California, Berkeley (US)
- Princess Margaret Cancer Centre (CA)
- Howard Hughes Medical Institute (US)
- Brown University (US)
- University of Washington (US)
- Corresponding author
- MacAlpine, David M.
- Strome, Susan
- Elgin, Sarah C. R.
- Liu, Xiaole Shirley
- Lieb, Jason D.
- Ahringer, Julie
- Karpen, Gary H.
- Park, Peter J.
- ORCID
- Ho, Joshua W. K.
- Jung, Youngsook L.
- Liu, Tao
- Lee, Soohyun
- Ikegami, Kohta
- Sohn, Kyung-Ah
- Minoda, Aki
- Tolstorukov, Michael Y.
- Parker, Stephen C. J.
- Gu, Tingting
- Kundaje, Anshul
- Riddle, Nicole C.
- Rechtsteiner, Andreas
- Asker, Dalal
- Belsky, Jason A.
- Chen, Q. Brent
- Chen, Ron A.-J.
- Epstein, Charles B.
- Ferrari, Francesco
- Garrigues, Jacob M.
- Gehlenborg, Nils
- He, Daniel
- Hoffman, Michael M.
- Jeffers, Tess E.
- Kharchenko, Peter V.
- Langley, Sasha A.
- Larschan, Erica N.
- Latorre, Isabel
- Libbrecht, Maxwell W.
- Lin, Xueqiu
- Pazin, Michael J.
- Qin, Bo
- Schwartz, Yuri B.
- Vielle, Anne
- Wang, Chengyang
- Xue, Huiling
- Kingston, Robert E.
- Kim, Ju Han
- Bernstein, Bradley E.
- Dernburg, Abby F.
- Kuroda, Mitzi I.
- Noble, William S.
- Tullius, Thomas D.
- Kellis, Manolis
- MacAlpine, David M.
- Strome, Susan
- Elgin, Sarah C. R.
- Ahringer, Julie
- Karpen, Gary H.
- Park, Peter J.
- Venue
- Nature
- Published
- 2014-08-27
- Volume
- 512
- Issue
- 7515
- Pages
- 449-452
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4227084
- OpenAlex
- W1981516407
- Cited by
- 390
- References
- 27
- Citations by year
- 2026: 6 · 2025: 13 · 2024: 21 · 2023: 30 · 2022: 25 · 2021: 58 · 2020: 24 · 2019: 42 · 2018: 31 · 2017: 45 · 2016: 35 · 2015: 49 · 2014: 11
- FWCI
- 19.12
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Nature (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Open Scholarship Institutional Repository (Washington University in St. Louis) (submittedVersion, cc-by-nc-sa)
- RePEc: Research Papers in Economics (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Science Foundation (1122374, 0000994)
- Howard Hughes Medical Institute
- Wellcome Trust (101863, 54523, 101863/Z/13/Z, 092096)
- National Natural Science Foundation of China (31028011, 1122374)
- National Institutes of Health (5u54hg004570-04, 1122374, U54-CA121852)
- National Human Genome Research Institute (U01HG004258, U01HG004270, K99HG006259, U01HG004279, U01HG004695, U54HG006991, U54-HG004570, R01HG004037, T32HG002295)
- National Cancer Institute (U54CA121852)
- National Institute of General Medical Sciences (T32GM071340, R01GM098461, R37GM048405)
- National Institute of Biomedical Imaging and Bioengineering (RL9EB008539)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Keywords
- chromatin organization, comparative genomics, histone modifications, repressive chromatin, heterochromatin, topologically associating domains, nucleosome positioning, DNA replication, enhancers, promoter, Caenorhabditis elegans, Drosophila melanogaster, human, modENCODE, ENCODE
- MeSH terms
- Animals, Cell Line, Centromere, Chromatin, DNA Replication, Drosophila melanogaster, Enhancer Elements, Genetic, Heterochromatin, Histones, Humans, Nucleosomes, Promoter Regions, Genetic, Species Specificity, Caenorhabditis elegans, Nuclear Lamina, Chromatin Assembly and Disassembly, Epigenesis, Genetic, Molecular Sequence Annotation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review